Circadian rhythms comprise oscillating molecular interactions, the disruption of the homeostasis of which would cause various disorders. To understand this phenomenon systematically, an accurate technique to identify oscillating molecules among omics datasets must be developed; however, this is still impeded by many difficulties, such as experimental noise and attenuated amplitude.
Iuchi et al BMC Bioinformatics (2018) 19:249 https://doi.org/10.1186/s12859-018-2257-4 RESEARCH ARTICLE Open Access MICOP: Maximal information coefficientbased oscillation prediction to detect biological rhythms in proteomics data Hitoshi Iuchi1,2, Masahiro Sugimoto2,3* and Masaru Tomita1,2,4 Abstract Background: Circadian rhythms comprise oscillating molecular interactions, the disruption of the homeostasis of which would cause various disorders To understand this phenomenon systematically, an accurate technique to identify oscillating molecules among omics datasets must be developed; however, this is still impeded by many difficulties, such as experimental noise and attenuated amplitude Results: To address these issues, we developed a new algorithm named Maximal Information Coefficient-based Oscillation Prediction (MICOP), a sine curve-matching method The performance of MICOP in labeling oscillation or non-oscillation was compared with four reported methods using Mathews correlation coefficient (MCC) values The numerical experiments were performed with time-series data with (1) mimicking of molecular oscillation decay, (2) high noise and low sampling frequency and (3) one-cycle data The first experiment revealed that MICOP could accurately identify the rhythmicity of decaying molecular oscillation (MCC > 0.7) The second experiment revealed that MICOP was robust against high-level noise (MCC > 0.8) even upon the use of low-sampling-frequency data The third experiment revealed that MICOP could accurately identify the rhythmicity of noisy one-cycle data (MCC > 0.8) As an application, we utilized MICOP to analyze time-series proteome data of mouse liver MICOP identified that novel oscillating candidates numbered 14 and 30 for C57BL/6 and C57BL/6 J, respectively Conclusions: In this paper, we presented MICOP, which is an MIC-based algorithm, for predicting periodic patterns in large-scale time-resolved protein expression profiles The performance test using artificially generated simulation data revealed that the performance of MICOP for decaying data was superior to that of the existing widely used methods It can reveal novel findings from time-series data and may contribute to biologically significant results This study suggests that MICOP is an ideal approach for detecting and characterizing oscillations in time-resolved omics data sets Keywords: Circadian rhythm, Mutual information, Proteomics Background The circadian rhythm, which involves oscillations over a cycle lasting 24-h, plays a critical role in biological systems [1] Transcriptional negative feedback loops composed of clock genes are a key component of this mechanism [1–3] These clock genes regulate downstream gene expression, leading to the 24-h cyclic * Correspondence: msugi@sfc.keio.ac.jp Institute for Advanced Biosciences, Keio University, Tsuruoka 997-0052, Japan Health Promotion and Preemptive Medicine, Research and Development Center for Minimally Invasive Therapies, Tokyo Medical University, Shinjuku, Tokyo 160-0022, Japan Full list of author information is available at the end of the article oscillation of various physiological phenomena such as cell division, energy metabolism, blood pressure, and sleep [4, 5] Many molecules are involved in these systems, so comprehensive and multilayered approaches are required to clarify the complex systems Thus, it is crucial to obtain a deep understanding of the circadian rhythm in order to understand biological systems The availability of biological time-course data is key to elucidating circadian rhythms, but there are several difficulties in analyzing biological time-series data In particular, the accumulation of time-series omics data via the technological innovation of mass spectrometry and DNA sequencers has led to the following problems: (1) low sampling frequency and (2) unstable oscillation The © The Author(s) 2018 Open Access This article is distributed under the terms of the Creative Commons Attribution 4.0 International License (http://creativecommons.org/licenses/by/4.0/), which permits unrestricted use, distribution, and reproduction in any medium, provided you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made The Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/) applies to the data made available in this article, unless otherwise stated Iuchi et al BMC Bioinformatics (2018) 19:249 first problem is derived from the generally low sampling frequency of omics datasets because comprehensive approaches such as proteomics and transcriptomics are often expensive and laborious Several omics studies collected time-course data every 2–4 h per day and estimated periodicity using 12 to 24 points [6–9] This sampling frequency of omics data was relatively low compared with those for locomotor activity or tissue luminescence, which were provided every minute [10] The second problem is the unstable oscillation (such as amplitude decay) of time-course experimental values There are various types of unstable oscillations in the expression pattern of genes and proteins For example, previous reports assumed unstable oscillations such as cosine with outlier time points, cosine with a linear trend, cosine with an exponential trend, and decaying cosine as possible natural oscillation phenomena [11, 12] These unstable oscillations hamper oscillation detection, in particular for amplitude decay, which is often observed in experimental systems and, is caused by degradation of the metabolic activity of cells and degradation of fluorescent protein [13] Therefore, novel computational analysis that functions over the time course of omics studies with limited sampling points and amplitude decay should be developed Many analytical approaches to predict molecules with oscillating levels from time-series data have been developed These algorithms were classified into time-domain and frequency-domain methods [14] Typical time-domain methods are based on cosine curve-based pattern matching and their simple algorithm helps biologists to evaluate their analytical results [14] For example, COSOPT and chi-squared periodogram are algorithms employing curve fitting and autocorrelation, respectively [15, 16] Hughes et al developed a nonparametric approach using rank by the nonparametric Jonckheere–Terpstra (JT) test and obtained the strength of correlation by Kendal’s tau test (JTK) [17] However, they have disadvantages, such as sensitivity to noise and outliers, and being able to detect only cosine wave-like curves; as such, there is a need for a novel algorithm that can overcome these obstacles Meanwhile, frequency-domain methods based on spectral analysis are strongly noise-resistant and model-independent [14] Fisher’s G-test estimates periodicity by calculating the periodogram of experimental data and calculating the P-value using Fisher’s G-statistic [18] Autoregressive spectral (ARS) analysis is an approach combining time-domain and frequency-domain methods, used to identify molecules with rhythmically oscillating levels in large-scale time-resolved profiles by autoregressive spectral analyses [19, 20] Similarly, an approach combining autocorrelation and spectral analysis after removing noise from raw data with a digital filter was also proposed [21]; however, frequency-domain methods are limited by the low sampling frequency and short time period in omics Page of 11 experiments, which means that they are often insufficient to predict the periodicity of large-scale omics datasets [22] Therefore, developed approaches to characterize oscillating molecules in biological data have been used with success and have contributed to our understanding of biological systems; meanwhile, it has been shown that each method sometimes produces inconsistent results because of noise, sampling rate, and waveform [23] A novel oscillation prediction method compatible with omics experiments, having a low sampling frequency, was required, for which quantitative evaluation of the performance could also be achieved This study developed Maximal Information Coefficient (MIC)-based Oscillating Prediction (MICOP) for analyzing time-series omics datasets with high-level noise and possible decay MICOP offers unsurpassed performance to identify and characterize oscillating molecules in omics datasets Methods Datasets Time-resolved data from biological samples are generally obtained every 2–6 h per day [6–9] Therefore, we simulated time-series data containing 6–24 points for two cycles for a performance test Half of these artificially simulated data did not feature oscillation, while the other half did For oscillating data, to mimic experimental data, noise according to the normal distribution (average = 0, standard deviation = 0–0.6) was added to the sin curve The decaying time-series datasets were designed so that the value of the peak in the second cycle is one-third of the value of the peak in the first cycle The nonoscillating data were random numerical data Proteomics datasets of C57BL/6 J and C57BL/6, which was already normalized, were downloaded from journal websites [8, 9] The simulated data released by Wu et al are included in MetaCycle, as described below [23, 24] Design A conceptual diagram of MICOP is shown in Fig The MIC belongs to the nonparametric exploration class, and the score indicates the strength of the linear or non-linear association between variables First, the mutual information for a scatterplot of X and Y is calculated as: I X; Y ị ẳ XX Y X pX; Y Þ log2 pðX; Y Þ pðX ÞpðY Þ Where p(X) and p(Y) are marginal probability distribution functions of X and Y, and p(X,Y) is joint probability distribution function Then, to compare the values from different grids and to obtain normalized values between Iuchi et al BMC Bioinformatics (2018) 19:249 a Page of 11 b Fig Concept of MICOP A conceptual diagram of MICOP is shown a Scheme of MICOP, b Typical results of MICOP Left boxes: experimental data (red) and reference sin curves (blue); right boxes: scatter plots between reference sin curve (x-axis) and experimental data (y-axis); top: typical oscillating data (MIC = 0.1, P < 0.05); middle: nonoscillating data (MIC = 0.22, P > 0.05); bottom: decaying oscillating data (MIC = 0.94, P < 0.05) and 1, MIC is divided by the lesser number of X and Y bins MIC is calculated as; MIC ðX; Y ị ẳ max X;Y MIC ðX; Y ÞÞ 1000 i¼1 where I is the indicator function, and Xpi and Ypi is the ith permutated version of X and Y, respectively If the datasets have missing points, MIC is calculated without the point Iuchi et al BMC Bioinformatics (2018) 19:249 Performance test To test the performance of MICOP, the periodicity of simulated data was determined by MICOP, JTK, ARS, and LS To compare the precision and sensitivity of MICOP, the MCC was compared [25] MCC values were calculated as below: TP Â TN−FP Â FN MCC ¼ pffiffiffiffiffiffiffiffiffiffiffiffiffiffiffiffiffiffiffiffiffiffiffiffiffiffiffiffiffiffiffiffiffiffiffiffiffiffiffiffiffiffiffiffiffiffiffiffiffiffiffiffiffiffiffiffiffiffiffiffiffiffiffiffiffiffiffiffiffiffiffiffiffiffiffiffiffiffiffiffiffiffiffiffiffiffiffiffi TP ỵ FP ịTP ỵ FN ịTN ỵ FP ịTN þ FN Þ where TP is the number of true positives, TN is the number of true negatives, FP is the number of false positives, FN is the number of false negatives The false discovery rate is widely used and is calculated from true positive and false positive values In contrast, MCC is more informative as a value evaluating the performance of the classification method because it is calculated from true positive, false positive, true negative, and false negative values Reanalysis of proteomics data To verify the practicality of MICOP, we reanalyzed the published time-series data [8, 9, 26] Briefly, these are proteome datasets of mouse liver sampled every h for days, and simulated data which are two cycles containing 20 molecules [26] The MIC and P-value were calculated as described in the Design section Programming language, packages, and statistical analysis R language (ver 3.3.2) was used for all analyses [27] Three different random seeds were used; rnorm function was used to generate random numbers according to a normal distribution and runif function was used to generate uniform random numbers The performance of each method was compared to MICOP by Tukey-Kramer test The P-values were corrected by the Benjamini–Hochberg procedure for multiple testing A graphical package named ggplot (ver 2.2.0) was used to draw figures The Minerva package (ver 1.4.3) was used to calculate the MIC score, and binning range to calculate MIC score was 0.6, which is a default value of the R library The MetaCycle package (1.1.0) was used for periodicity judgment by ARS, JTK, and LS [21, 23, 24] Results Comparison of MICOP and existing methods for decaying data To test the performance of MICOP, JTK, ARSER, and Lomb-Scargle (LS) for mimicking the decaying time-resolved data, the Matthews correlation coefficient (MCC) values were calculated to differentiate significantly oscillating data from nonoscillating data using time-series simulation data, including 100 sets of oscillating data and 100 sets of nonoscillating ones (Fig 2, Additional file 1) [17, 20] Two-way ANOVA with Method and sampling frequency as factors revealed Page of 11 significant effects of Method (F = 631.8, P < 0.005), sampling frequency (F = 810.1, P < 0.005) and Method x sampling frequency interaction (F = 122.9, P < 0.005) MCC values were 0.72 (P < 0.005), 0.40 (P < 0.005), 0.082 (P < 0.005), and 0.00 (P < 0.005) for MICOP, ARS, JTK, and LS, respectively, when the sampling interval was h (Fig 2) The MCC values increased as the sampling frequency increased, and these values became almost equal to in all methods at 1-h interval sampling The MCC values of MICOP were 0.7 or more at all sampling frequencies and were the highest at a sampling interval of 1–3 h, followed by ARS and JTK LS did not function as a classifier at a sampling interval of 1–3 h Comparison of MICOP and existing methods for noisy or low-sampling-frequency or one-cycle data We compared the accuracy of MICOP and existing methods for time-series data containing noise and having a low sampling frequency without attenuation (Fig 3a and b, Additional file 2) Initially, we quantitatively evaluated the degradation of classification performance due to the noise of MICOP (Fig 3a) Two-way ANOVA with Method and noise level as factors revealed significant effects of Method (F = 1099.4, P < 0.005), noise level (F = 643.2, P < 0.005) and method x noise level interaction (F = 475.5, P < 0.005) The MCC values were 0.8 or more, except for LS, in all conditions, even if the noise was 0.500; however, LS did not function as a classifier when the noise was 0.375 or more The performance of MICOP as a classifier for low-sampling-frequency unattenuated data was also quantitatively evaluated (Fig 3b) Two-way ANOVA with Method and sampling frequency as factors revealed significant effects of Method (F = 424.3, P < 0.005), sampling frequency (F = 447.7, P < 0.005) and Method x sampling frequency interaction (F = 142.2, P < 0.005) The MCC values increased in all methods as the sampling interval decreased, and were equal to in all four methods at a sampling interval of h LS did not function as a classifier at sampling intervals of 3–4 h The MCC values of MICOP were 0.7 or more under all conditions We compared the accuracy of MICOP and existing methods for one-cycle data (Fig 4) Among all conditions (method, noise, and sampling frequency), determination accuracies using one-cycle were lower than those using two cycles All methods did not work under all conditions at the 4-h sampling frequency Meanwhile, MICOP and JTK showed high performances under sampling conditions ≤3 h Reanalysis of previously reported time-resolved proteomics datasets We reanalyzed the time-series proteome data for mouse liver reported by Mauvoisin et al using C57BL/6 and Iuchi et al BMC Bioinformatics (2018) 19:249 Expression a Page of 11 Typical decaying oscillation b 1.5 1.0 1.0 0.0 0.5 Typical non-oscillation -1.0 0.0 -2.0 10 20 30 40 50 Time 10 20 30 40 50 Time c 1.00 MCC value 0.75 *** *** *** *** *** *** *** * MICOP ARS JTK LS 0.50 0.25 * : P < 0.05 ** : P < 0.01 *** : P < 0.005 0.00 Sampling interval (hours) Fig MCC values of MICOP, ARS, JTK, and LS for decaying data Comparison of detection power of MICOP and existing methods for decaying data a Typical decaying oscillation data, b typical non-oscillation data, c MCC values from simulated time-resolved data in which half represent oscillating data, whereas the other half represent random numerical data, of which half not oscillate Noise level was 0.4 (standard deviation) The x-axis represents the MCC value, while the y-axis represents the sampling interval (hours) The color indicates each method: red, MICOP; green, ARS; blue, JTK; and purple, LS those reported by Robles et al using C57BL/6 J, as well as simulated data released by Wu et al (Fig 5, Table 1, Table 2) [8, 9, 23] The numbers of significantly oscillating proteins assessed by standard harmonic regression were (the F test for multilinear regression, P < 0.01), (Fisher’s exact test, P < 0.01), and (P < 0.01) for biological data in the original work Meanwhile, 32, 22, and proteins were judged as being significantly oscillating for C57BL/6 J, C57BL/6, and Wu’s simulated data by MICOP, respectively (P < 0.05) The numbers of proteins judged to be significantly oscillating in both the original work and MICOP were 2, 8, and for biological data, respectively The numbers of proteins judged as being significantly oscillating for the three above-mentioned tests only by MICOP were 30, 14, and for biological data, respectively Discussion Although many algorithms have been developed to extract molecules with rhythmic oscillation in their levels from large-scale time-series data derived from mass spectrometry systems or DNA sequencers, it is known that the accuracy and sensitivity of such methods depend on noise, sampling frequency, and waveform In particular, the discussion of the prediction power in conditions of decaying oscillation was insufficient In this research, we provide MICOP, which is classified as a time-domain method, and demonstrate that the algorithm is particularly effective for detecting decaying oscillation We compared the detection power of MICOP and previously reported algorithms for decaying oscillation We revealed that, in terms of the power for detection decaying oscillation, MICOP outperformed other algorithms (Fig 2) In particular, MICOP showed a clear advantage when the sampling frequency was low This is because MIC can effectively detect non-linear associations like associations between decaying oscillation and the reference sin curve (Fig 1) Although we compared the performance for only cosine wave, additional experiment with peak wave or complex wave is also important ARS showed high performance following MICOP because de-trending at preprocessing seemed to cancel out Iuchi et al BMC Bioinformatics (2018) 19:249 Page of 11 a a *** b *** MCC value 1.00 0.75 MICOP ARS JTK LS 0.50 0.25 0.00 0.125 0.25 0.375 0.5 Noise * : P < 0.05 ** : P < 0.01 *** : P < 0.005 c b *** 1.00 MCC value *** 0.75 0.50 Fig Venn diagrams of significant molecules the levels of which oscillate Published time-resolved data sets were reanalyzed by MICOP, and Venn diagrams were constructed to quantify the overlap between MICOP and the original article a and b represent mouse proteomics data: a C57BL/6 J [9], b C57BL/6 [8], and c Wu’s simulated data [23] Blue indicates original article and green indicates MICOP P-values were calculated by Chi-square tests to analyze overlap between MICOP and the original research article 0.25 0.00 sampling interval (hours) Fig MCC values for time-series data with different sampling frequencies or gradually added noise without attenuation Comparison of MCC values of each method when noise was added gradually (3-h sampling frequency) (a) and when the sampling frequency was changed (noise level was 0.4) (b), and both simulation data sets were not decaying The P-value calculated by Tukey-Kramer test The error bar indicates standard deviation (n = 3) the decay of time-series data JTK was the tool with the third best detection power, although high performance was expected because it was based on Kendall’s tau, which is a measure of rank correlation, and it did not depend on amplitude This indicates that MICOP has Sampling frequency 1.00 0.50 0.125 0.00 1.00 0.50 MCC 0.25 0.50 MICOP ARS JTK LS 0.375 0.00 1.00 Noise level 0.00 1.00 0.50 0.00 1.00 0.5 0.50 MICOP ARS JTK LS MICOP ARS JTK LS MICOP ARS JTK LS MICOP ARS JTK LS 0.00 Fig MCC values for time-series data with one-cycle data Comparison of MCC values for each method with one-cycle time-series data Row order indicates noise level and column order indicates sampling interval (h) Colors refer to each method Sampling frequency and noise level were gradually adjusted Iuchi et al BMC Bioinformatics (2018) 19:249 Page of 11 Table Novel oscillating protein candidates of C57BL/6 J [9] detected by MICOP Gene name Species Condition Tissue Reference Acot8 – – – – Acox1 Homo sapiens LL blood [36] Mus musculus LD liver/SCN [37, 38] Acsl5 Mus musculus DD/LD liver/SCN [39] Mus musculus LD SCN [37] Akr1c14 Mus musculus LD liver [40] Mus musculus DD cartilage tissue [41] Cbs Mus musculus DD/LD liver [42–45] Mus musculus LD SCN [37] Homo sapiens LL blood [36] Cct8 Mus musculus LD SCN [37] Ces1b – – – – Chid1 Mus musculus DD/LD liver/SCN [46] Cxadr Mus musculus DD/LD liver/SCN [42] Cyp4f14 – – – – Gns Homo sapiens LL blood [36] Mus musculus DD/LD liver [40] Golgb1 Mus musculus DD/LD liver/SCN [37, 40, 47] Gpx3 – – – – Hars Mus musculus LD liver [40] Hrg – – – – Mfap4 – – – – Mug1 Mus musculus DD liver [42] Pdcd6 Mus musculus LD liver/SCN [37, 40, 47], Ptms Mus musculus LD SCN [37] Safb – – – – Serpina6 Mus musculus DD/LD liver [44] Sf3b2 Mus musculus LD telogen epidermis [46] Slc9a3r1 Mus musculus DD/LD liver [46] Snrpd3 Mus musculus LD liver [47] Stk38 Mus musculus DD liver [46] Mus musculus LD SCN [37] Tpr Mus musculus DD/LD liver [40, 46] Txndc15 Mus musculus DD/LD liver [46, 47] Mus musculus LD SCN [37] Ubl4a Mus musculus LD SCN [37] Mus musculus DD liver [46] Uox Mus musculus DD/LD liver [39, 40, 42, 47] Ythdf2 Mus musculus LD liver [47] Novel oscillating protein candidates identified by MICOP from time-series proteomics data of C57BL/6 J [9] and a list of previous papers that have experimentally demonstrated that gene expression oscillates in transcriptome analysis LD stands for the daily 24-h light-dark (LD) cycle and DD stands for constant darkness conditions Hyphens indicate that we could not find previous consistent works which prove the mRNA oscillation Iuchi et al BMC Bioinformatics (2018) 19:249 Page of 11 Table Novel oscillating protein candidates of C57BL/6 [8] detected by MICOP Gene name Species Condition Tissue Reference Anp32e Mus musculus DD/LD liver [39, 40] Anpep – – – – Cgn Mus musculus LD liver [47] Csde1 Mus musculus DD liver [39] Mus musculus LD SCN [37] Enpp4 Mus musculus LD liver/anagen epidermis [40, 46, 47] Gnl2 Mus musculus DD hippocampus/liver [39, 48] Mus musculus LD SCN [37] Ldhb Numa1 Homo sapiens LL blood [36] Mus musculus LD anagen epidermis, SCN [37, 46] Mus musculus LD liver [40] Mus musculus DD cartilage tissue [41] Prdx2 Mus musculus LD SCN [37] Rnf114 – – – – Slc4a1 – – – – Slco1b2 Mus musculus DD/LD liver [39, 40, 42] Tomm70a – – – – Vps26a – – – – Novel oscillating protein candidates identified by MICOP from time-series proteomics data of C57BL/6 [8] and a list of previous papers which experimentally demonstrated that gene expression oscillates in transcriptome analysis LD stands for the daily 24-h light-dark (LD) cycle and DD stands for constant darkness conditions Hyphens indicate that we could not find previous consistent works which prove the mRNA oscillation excellent performance for decaying oscillation, and suggests that an MIC-based approach that can detect non-linear associations is useful to detect decaying oscillation Moreover, we compared the MCC values for all methods on data containing gradual Gaussian noise to test the noise resistance (Fig 3a) As a result, MICOP showed equal performance to JTK and ARS in the range of standard deviation of 0.125–0.500 This indicated that the performance of MICOP for noisy data is equal to that of the existing methods This result suggests that the robustness to noise of MICOP is the same as that of well-known ARS and JTK, while the high performance of LS was limited to conditions with a low noise level This numerical experiment revealed that the noise resistance of MICOP is the same as that of other widely used methods Clarifying the relationship between accuracy and sampling frequency in analyzing omics data, for which increasing the number of sampling points seems difficult, is important for determining the experimental design As expected, with increase in the sampling frequency, the MCC values tended to increase (Figs and 3b) The fact that the ARS, JTK, and LS could characterize oscillation and non-oscillation in almost all cases when the sampling interval was h or less is similar to the findings in original research studies of various methods and research comparing them [11, 28] This suggested that a high sampling frequency improved accuracy; therefore, sampling frequency should be as high as experimental constraints allow We applied MICOP and existing methods for one-cycle of data (Fig 4) As expected, accuracy decreased for all methods when one-cycle was used However, MICOP and JTK showed high MCC values among methods under this condition Also, MICOP seems to outperformed JTK under limited conditions which is low sampling frequency and high noise for one-cycle data (Fig 4) Human omics data often have lower sampling frequencies, high noise levels, and only one-cycle Our results suggest that MICOP and JTK have considerable potential for analyzing human omics datasets We reanalyzed the time-series proteomics data of C57BL/6 J and C57BL/6 to test the performance of MICOP and explore additional candidates of proteins with rhythmic change in their expression profile [8, 9] These datasets include the mouse liver proteome data obtained by sampling every h for days, for which the analysis of the peptides was performed with a mass spectrometer Approximately, 3000 protein types were detected in each study Proteins that were detected in both MICOP and the original studies numbered and for C57BL/6 J and C57BL/6, respectively (Fig 5) This actual application for proteomics data suggests that MICOP can obtain results in a manner approximately similar to Iuchi et al BMC Bioinformatics (2018) 19:249 the existing methods Specifically, the MICOP results were consistent with those in the original articles regarding these commonly identified proteins Furthermore, the proteins that were uniquely identified with MICOP were numbered 30 and 14 for C57BL/6 J and C57BL/6, respectively (Table 1, Table 2) These results strongly suggest that MICOP is a powerful tool to detect proteins with rhythmic changes in their expression levels from time-resolved proteomics data Although mass spectrometry-based approaches have been used for proteome-level studies of circadian rhythms, completely measuring mouse proteomes remains difficult A comprehensive transcriptome analysis with parallel sequencers has revealed that ~ 15–20% of mouse liver mRNA significantly oscillates [29] However, in these proteome studies of C57BL/6 and C57BL/6 J, significantly oscillating protein are rare (< 1% of detected total proteins; FDR < 0.05), a result inconsistent with those of mouse proteome studies Multiple factors can explain this pattern Typical clock protein known as principle oscillators such as CRY1, CRY2, PER2, REV-ERBα and CLOCK have comparatively low expression levels and are not detected in these studies [8, 9] In addition, non-Gaussian experimental noise which is specific to MS measurement hampers the application of statistical test on proteins [30] These problems may be improved by analyzing higher quality proteome datasets with modern technologies [31, 32] Some core circadian proteins such as CRY1, CRY2, PER2, REV-ERVα and CLOCK could be detected in recently published proteome datasets [31, 32] Thus, the development of proteome analysis technology may resolve discrepancies between results of transcriptome analysis and proteome analysis, and clarify connections within the circadian rhythm transcription and translation network We present a new list of proteins that oscillate by MICOP (Tables and 2) The accuracy of these estimates is difficult to ascertain Interestingly, when examining expression patterns of genes encoding these proteins, we estimated that the proteins were new oscillating molecules in MICOP In addition, a large fraction of candidates was presumed to oscillate in a previous transcriptome analysis [29] Two independent studies which measured both transcriptome and proteome of human samples revealed that only 30% of mRNA-protein correlation had statistically significant [33, 34] This fact suggested that even if mRNA abundance is oscillating, protein abundance may not be always oscillating However, about 90% of mRNA-protein correlation showed positive, hence rhythmic mRNA expression suggests the possibility of protein oscillation [34] An overlap between re-analyzed proteomics data by MICOP and transcriptome analysis showed a consistent result Page of 11 MICOP accuracy tends to be low for data that not perfectly fit a sine curve The periodicity that MICOP can detect is subject to the shape of the reference curve, so changing the reference curve is necessary to detect asymmetric waveforms including saw tooth-like shapes like RAIN [30] Furthermore, adjusting the false discovery rate is essential for accurate prediction, since MICOP repeats the hypothesis tests In addition, verification with additional data such as periodic peak wave or overlapping sine wave is necessary in order to evaluate the accuracy of MICOP more precisely Judgments of phase and cycle are possible in principle, but we did not perform them; therefore, this should be considered in future studies Mutual information increased when sample size was small and correlation between two variables was null, even when the variables were random [35] We solved this issue in MICOP by determining the P-value with the Monte Carlo method When the time points (sample size) are small, the criterion for calculating the P-value increases, and when the time points are large, the criterion for calculating the P-value decreases (Additional file 3) In this paper, we presented MICOP, which is an MIC-based algorithm, for predicting periodic patterns in large-scale time-resolved protein expression profiles The performance test using artificially generated simulation data revealed that the performance of MICOP for decaying data was superior to that of the existing widely used methods Additionally, we indicated that MICOP is compatible with noisy data obtained with a low sampling frequency Furthermore, the performance test using actual mouse proteomics data suggested that MICOP may be able to provide novel findings from proteomics data Specifically, it can reveal novel findings from time-series data and may contribute to biologically significant results This study suggests that MICOP is an ideal approach for detecting and characterizing oscillations in time-resolved omics data sets Conclusion In this paper, we presented MICOP, which is an MIC-based algorithm, for predicting periodic patterns in large-scale time-resolved protein expression profiles The performance test using artificially generated simulation data revealed that the performance of MICOP for decaying data was superior to that of the existing widely used methods Additionally, we indicated that MICOP is compatible with noisy data obtained with a low sampling frequency Furthermore, the performance test using actual mouse proteomics data suggested that MICOP may be able to provide novel findings from proteomics data Specifically, it can reveal novel findings from time-series data and may contribute to biologically significant results This study suggests that MICOP is an ideal approach for detecting and characterizing oscillations in time-resolved omics data sets Iuchi et al BMC Bioinformatics (2018) 19:249 Additional files Additional file 1: Wide range comparison of MCC values of MICOP, ARS, JTK, and LS for decaying data Sampling interval and noise level were gradually adjusted The bar indicates MCC values (1 indicates a perfect prediction, indicates a random prediction, and − indicates a prediction in complete disagreement) (PDF 75 kb) Additional file 2: Wide-range comparison of MCC values of MICOP, ARS, JTK, and LS for non-decaying data Sampling interval and noise level were gradually adjusted The bar indicates MCC values (1 indicates a perfect prediction, indicates a random prediction, and − indicates a prediction in complete disagreement) (PDF 75 kb) Additional file 3: Monte-Carlo simulation to calculate P-values MIC values were calculated between random numbers The x-axis indicates sample number (N time points) and the y-axis indicates MIC The error bar indicates the standard deviation (N = 1000) The red color represents random values and the blue color represents the significance threshold (5%) (PDF 68 kb) Abbreviations ARS: Autoregressive spectral estimation; FN: False Negative; FP: False positive; JTK: Jonckheere–Terpstra (JT) test and obtained the strength of correlation by Kendal’s tau test; LS: Lomb-Scargle; MCC: Mathews correlation coefficient; MIC: Maximal information coefficient; MICOP: Maximal information coefficient-based oscillation prediction; MINE: Maximal information-based nonparametric estimation; TN: True negative; TP: True positive Funding This work was supported by research funds from the Yamagata Prefectural Government and by research funds from Tsuruoka City, Japan Availability of data and materials The scripts for analysis were uploaded on the following URL https:// docs.google.com/document/d/ 1bN44qAJFP9O6BTTA_0ameil9py0LS3rcXKT2cxbKTwY/edit?usp=sharing Authors’ contributions HI conducted the bioinformatics analyses MS supervised the project HI and MS wrote the manuscript MT supported the writing of the manuscript All authors have read and approved the final manuscript Page 10 of 11 10 11 12 13 14 15 Ethics approval and consent to participate Not applicable 16 Consent for publication Not applicable 17 Competing interests The authors declare that they have no competing interests 18 19 Publisher’s Note Springer Nature remains neutral with regard to jurisdictional claims in published maps and institutional affiliations 20 Author details Systems Biology Program, Graduate School of Media and Governance, Keio University, Fujisawa 252-8520, Japan 2Institute for Advanced Biosciences, Keio University, Tsuruoka 997-0052, Japan 3Health Promotion and Preemptive Medicine, Research and Development Center for Minimally Invasive Therapies, Tokyo Medical University, Shinjuku, Tokyo 160-0022, Japan 4Department of Environment and Information Studies, Keio University, Fujisawa 252-8520, Japan 21 22 23 24 Received: 12 October 2017 Accepted: 20 June 2018 25 References Mohawk JA, Green CB, Takahashi JS Central and peripheral circadian clocks in mammals Annu Rev Neurosci 2012;35:445–62 26 Koike N, Yoo SH, Huang HC, Kumar V, Lee C, Kim TK, Takahashi JS Transcriptional architecture and chromatin landscape of the core circadian clock in mammals Science 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Mathews correlation coefficient; MIC: Maximal information coefficient; MICOP: Maximal information coefficient-based oscillation prediction; MINE: Maximal information- based nonparametric estimation;... sampling frequency in analyzing omics data, for which increasing the number of sampling points seems difficult, is important for determining the experimental design As expected, with increase in. .. is difficult to ascertain Interestingly, when examining expression patterns of genes encoding these proteins, we estimated that the proteins were new oscillating molecules in MICOP In addition,